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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067511Generated: October 25, 2026

Sodium hydride → 6-[2-[2-[4-(Diphenylmethyl)piperazino]ethoxy]ethoxy]-7-methyl[1,2,4]triazolo[1,5-b]pyridazine

https://huagongshe.com/reaction/1067511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDecloxizineHCID 71135—
Reactant6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazineHCID 11805158—
SolventTetrahydrofuranHCID 8028—
Product6-[2-[2-[4-(Diphenylmethyl)piperazino]ethoxy]ethoxy]-7-methyl[1,2,4]triazolo[1,5-b]pyridazineHCID 2298938248.2%

Reaction Steps

260 mg of 60% sodium hydride dispersion in mineral oil was suspended in 20 ml of tetrahydrofuran; 1.15 g of 4-(diphenylmethyl)-1-[2-(2-hydroxyethoxy)ethyl]piperazine was added, followed by heating and refluxing for 1 hour. After cooling, 540 mg of 6-chloro-7-methyl[1,2,4]triazolo[1,5-b]pyridazine was added, followed by heating and refluxing for 3 hours. After cooling, ice water was added, followed by extraction with ethyl acetate; the extract was washed with saturated saline and dried with magnesium sulfate. After the dry product was concentrated under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with dichloromethane-ethyl acetate-methanol (10:10:1). The desired fraction was collected; the crystal precipitated was collected by filtration, washed with ethyl ether and dried to yield 730 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248740B1
Source datasetuspto-grants-2001_06
ORD IDord-4d18ddf017224ddfa93ab79630c5e025
Source noteuspto-grants-2001_06